Clinical Research Coordinator II - Tacoma WA

present of AI; Tacoma (WA); On-site; USD 65,000 - 80,000; Full time

Job summary

Iterative Health in Tacoma, WA seeks a Clinical Research Coordinator II to run industry-sponsored trials from startup to closeout at a community site. A strong candidate has hands-on research or healthcare experience, follows protocols, keeps clean records, and handles visits, specimens, and patient questions with care.

The role supports recruitment and consent discussions, manages multiple priorities, and works with digital trial tools to streamline screening and data checks, while maintaining

Qualifications

• Hands-on experience in clinical research settings or healthcare, familiar with protocols and data systems.
• Ability to support patient recruitment and consent processes.
• Attention to data quality and regulatory requirements throughout trials.

Responsibilities

• Coordinate patient visits, procedures, and sample collection per protocol.
• Conduct informed consent discussions and answer participant questions.
• Maintain accurate source documents and trial records in CTMS/EDC.
• Communicate with sponsors and monitors and address trial-related issues.

Skills

Clinical research

Patient recruitment

Data entry

Regulatory compliance

Tools

CTMS

EDC systems

Spreadsheets

Job description

Clinical Research Coordinator II - Tacoma WA

This role runs industry sponsored trials largely on its own, from startup through closeout, at a community site. A strong candidate has several years of hands on research or healthcare work, can follow a protocol closely, keeps clean records in tracking and data systems, and handles visits, specimens, and patient questions with care. Comfort with recruitment, consent conversations, and juggling several priorities at once matters more than supervision.

How it fits the AI era

The company pairs trial work with AI, so some screening, tracking, and data checks likely lean on software, freeing time for patient visits and judgment calls. The human core stays: consent discussions, clinical procedures, safety review, and keeping sponsors and monitors informed. A coordinator who works well with digital tools and still catches what a system misses fits this setting.

How it builds AI experience

Experience would come from using trial management and data capture systems daily and learning how AI assisted screening or enrollment tools support site goals. Building it means getting fluent in those platforms and understanding how data quality feeds downstream review. Familiarity with the company's focus areas in digestive, liver, heart, and obesity research would help.

Worth showing

• Protocol and GCP compliance
• Patient recruitment and consent
• CTMS and EDC systems
• Specimen handling and phlebotomy

This is our own read, written from the employer's posting and the company's Spotlight. The employer's posting is the source of truth for the role.

About Iterative Health

Iterative Health embeds clinical research into community care settings, and per the company, runs trials 2x faster to activate sites and 3x higher patient enrollment.